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Acetarsone - 96%, high purity , CAS No.97-44-9

COA COA
    Grade & Purity:
  • ≥96%
  • Cas Number:  97-44-9
  • Molecular Weight:  275.09
  • PubChem CID: 1985
In stock
Item Number
A357000
Grouped product items
SKU Size
Availability
 Price Qty
A357000-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$103.90
A357000-250mg
250mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$344.90
A357000-1g
1g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$996.90
A357000-5g
5g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$3,434.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet

an antiifective agent used as an antiprotozoal

View related series
Parasite (997)

Basic Description

Synonyms Acetarsolo [DCIT] | Ehrlich 594 | DTXCID7025847 | HMS500A04 | Osvarsan | Paroxyl | SPBio_000088 | 3-Acetamido-4-hydroxybenzenearsonic acid | EINECS 202-582-3 | NSC 13160 | Acetarsolum | Acetarsolum [INN-Latin] | Acetphenarsine | HMS3371H07 | KBioGR_000907
Specifications & Purity ≥96%
Storage Temp Room temperature
Shipped In Normal
Product Description

Application：

Acetarsone is an antiifective agent used as an antiprotozoal.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Anilides
Intermediate Tree Nodes Not available
Direct Parent Acetanilides
Alternative Parents N-acetylarylamines  1-hydroxy-2-unsubstituted benzenoids  Pentaorganoarsanes  Acetamides  Secondary carboxylic acid amides  Oxygen-containing organoarsenic compounds  Organic metalloid salts  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Acetanilide - N-acetylarylamine - N-arylamide - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Pentaorganoarsane - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Oxygen-containing organoarsenic compound - Organic metalloid salt - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organoarsenic compound - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as acetanilides. These are organic compounds containing an acetamide group conjugated to a phenyl group.
External Descriptors Not available

Associated Targets(Human)

POLB Tchem DNA polymerase beta (23632 Activities)
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A498 (42825 Activities)
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ACHN (49357 Activities)
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CAKI-1 (44928 Activities)
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CCRF-CEM (65223 Activities)
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COLO 205 (50209 Activities)
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DU-145 (51482 Activities)
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HL-60 (67320 Activities)
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HT-29 (80576 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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M14 (47487 Activities)
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MCF7 (126967 Activities)
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MOLT-4 (49676 Activities)
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OVCAR-3 (48710 Activities)
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OVCAR-4 (44535 Activities)
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OVCAR-5 (45555 Activities)
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OVCAR-8 (47708 Activities)
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PC-3 (62116 Activities)
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RPMI-8226 (44974 Activities)
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RXF 393 (41971 Activities)
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SF-295 (48000 Activities)
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SK-MEL-2 (46422 Activities)
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SK-MEL-28 (48833 Activities)
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SK-MEL-5 (47095 Activities)
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SK-OV-3 (52876 Activities)
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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
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TK-10 (45540 Activities)
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U-251 (51189 Activities)
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UACC-257 (46019 Activities)
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UACC-62 (47335 Activities)
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UO-31 (46270 Activities)
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786-0 (47912 Activities)
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A549 (127892 Activities)
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NCI/ADR-RES (33767 Activities)
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T47D (39041 Activities)
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EKVX (44102 Activities)
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NCI-H322M (45589 Activities)
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HCC 2998 (41480 Activities)
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HCT-116 (91556 Activities)
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HOP-92 (41141 Activities)
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Hs-578T (29457 Activities)
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NCI-H460 (60772 Activities)
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SF-268 (49410 Activities)
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IGROV-1 (47897 Activities)
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LOX IMVI (44321 Activities)
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HOP-62 (47048 Activities)
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MDA-MB-435 (38290 Activities)
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MDA-N (28205 Activities)
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Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
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Pseudomonas aeruginosa (123386 Activities)
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Klebsiella pneumoniae (43867 Activities)
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Staphylococcus aureus (210822 Activities)
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Acinetobacter baumannii (41033 Activities)
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Escherichia coli (133304 Activities)
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Plasmodium falciparum (966862 Activities)
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Cryptococcus neoformans (21258 Activities)
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Candida albicans (78123 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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pfk 6-phospho-1-fructokinase (7870 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
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SARS-CoV-2 (38078 Activities)
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Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name (3-acetamido-4-hydroxyphenyl)arsonic acid
INCHI InChI=1S/C8H10AsNO5/c1-5(11)10-7-4-6(9(13,14)15)2-3-8(7)12/h2-4,12H,1H3,(H,10,11)(H2,13,14,15)
InChIKey ODFJOVXVLFUVNQ-UHFFFAOYSA-N
Smiles CC(=O)NC1=C(C=CC(=C1)[As](=O)(O)O)O
Isomeric SMILES CC(=O)NC1=C(C=CC(=C1)[As](=O)(O)O)O
UN Number 3465
Packing Group II
Molecular Weight 275.09
Reaxy-Rn 2941984
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2941984&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Solubility insoluble in H2O; insoluble in EtOH; ≥12.95 mg/mL in DMSO with gentle warming
Melt Point(°C) 225-227° C
Molecular Weight 275.090 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 2
Exact Mass 274.977 Da
Monoisotopic Mass 274.977 Da
Topological Polar Surface Area 107.000 Ų
Heavy Atom Count 15
Formal Charge 0
Complexity 289.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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